Canonical Allele Identifier: CA555318049

Gene: IL15

Linked Data

• dbSNP Id: rs1278851832
• gnomAD v2: 4-142654294-GTGT-G
• gnomAD v3: 4-141733141-GTGT-G
• gnomAD v4: 4-141733141-GTGT-G
• MyVariant Identifiers: chr4:g.142654295_142654297del (hg19) ; chr4:g.141733142_141733144del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733146_141733148del , CM000666.2:g.141733146_141733148del	GRCh38
NC_000004.11:g.142654299_142654301del , CM000666.1:g.142654299_142654301del	GRCh37
NC_000004.10:g.142873749_142873751del	NCBI36
NG_029605.1:g.101551_101553del
NG_029605.2:g.101551_101553del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*298_*300del MANE Select	ENSP00000323505.4:n.*298_*300del
ENST00000296545.11:c.*298_*300del	ENSP00000296545.7:n.*298_*300del
ENST00000320650.8:c.*298_*300del	ENSP00000323505.4:n.*298_*300del
ENST00000394159.2:c.706_708del	ENSP00000377714.1:n.706_708del
ENST00000477265.5:c.*298_*300del	ENSP00000436914.1:n.*298_*300del
ENST00000514653.5:c.*298_*300del	ENSP00000422271.1:n.*298_*300del
NM_000585.4:c.*298_*300del	NP_000576.1:n.*298_*300del
NM_172175.2:c.*298_*300del	NP_751915.1:n.*298_*300del
NR_037840.2:n.1637_1639del
NM_000585.5:c.*298_*300del MANE Select	NP_000576.1:n.*298_*300del
NM_172175.3:c.*298_*300del	NP_751915.1:n.*298_*300del
NR_037840.3:n.1650_1652del